MotoBAND™ CP DynaForce® MPJ 7R50-0018Recalls & reported problems
Crossroads Extremity Systems · The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00815432025015), received between Mar 22, 2019 and Mar 22, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (1 report).
1 other recall cover devices cleared under the same FDA submission (K173710); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Break1
- Mechanical Problem1
Patient problems
- Nonunion/Delayed-union Bone Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 22, 2019Break; Mechanical Problem
3 MONTH ROUTINE POST OP FOLLOW UP VISIT REVEALED FAILURE OF THE MOTOBAND CP IMPLANT SYSTEM TO PROVIDE ADEQUATE FUSION AT THE FUSION SITE DUE TO BROKEN HARDWARE. DYNAFORCE STAPLE IMPLANT EXPERIENCED MECHANICAL FAILURE IN BOTH LEGS. ADDITIONALLY, ONE OF THE SCREWS EXPERIENCED MECHANICAL FAILURE AS WELL. THE DOCTOR STATED THE PATIENT WAS NON-COMPLIANT. THE JOINT WILL BE REVISED BUT A REVISION DATE HAS NOT BEEN SCHEDULED. X-RAY IMAGE WILL BE INCLUDED.
Patient problems: Nonunion/Delayed-union Bone Fracture
MAUDE report 8443484 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K173710. One submission often covers many models, so check the product and lot details in each record.
- Z-0212-2020 · Sep 19, 2019 · TerminatedMotoBand CP, Poly-axial Locking Screw, 3.0mm x 28mm
Other Plate, Fixation, Bone devices
- Lapiplasty System 2 SK14Treace Medical Concepts, Inc. · Plate, Fixation, Bone260 reports
- PRECICE® Plating System LP4.5-PRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls6 reports
- PRECICE® Plating System LP4.5-MLT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls5 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-MLT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-MRT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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